Literature DB >> 7513419

Infantile systemic hyalinosis in a black infant.

E E Sahn1, C F Salinas, M A Sens, J Key, F K Swiger, K A Holbrook.   

Abstract

A black girl was born with flexion contractures and experienced pain on movement by 1 week of age. She subsequently developed perioral papules, gingival hyperplasia, perianal nodules, torticollis, diarrhea, rectal prolapse, and inability to open her mouth. Her skin became increasingly sclerodermatous, and velvety, hyperpigmented plaques arose over bony prominences. A skin biopsy specimen showed hyaline material in the papillary dermis with lack of elastic fibers. Ultrastructural examination revealed fibrillogranular material around fibroblasts and blood vessels. This child had the clinical, histologic, and ultrastructural features of infantile systemic hyalinosis. This disorder has not been described in a black infant. Previous case reports of infantile systemic hyalinosis are reviewed and unusual features of our case are discussed.

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Year:  1994        PMID: 7513419     DOI: 10.1111/j.1525-1470.1994.tb00076.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  7 in total

1.  Infantile systemic hyalinosis: report of three Iranian children and review of the literature.

Authors:  Yahya Aghighi; Shahla Bahremand; Laleh Razavi Nematollahi
Journal:  Clin Rheumatol       Date:  2005-12-03       Impact factor: 2.980

2.  Clinical and imaging findings of systemic hyalinosis: two cases presenting with congenital arthrogryposis.

Authors:  So-Young Yoo; Ji Hye Kim; Ho Seok Kang; Yong Seung Hwang; Ki Joong Kim; In-One Kim; Jung-Eun Cheon; Su-Mi Shin; Chong Jai Kim; Jee Hun Lee; Mun Hyang Lee; Jong Hee Chae
Journal:  Skeletal Radiol       Date:  2010-02-06       Impact factor: 2.199

3.  Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis.

Authors:  Sandra Hanks; Sarah Adams; Jenny Douglas; Laura Arbour; David J Atherton; Sevim Balci; Harald Bode; Mary E Campbell; Murray Feingold; Gökhan Keser; Wim Kleijer; Grazia Mancini; John A McGrath; Francesco Muntoni; Arti Nanda; M Dawn Teare; Matthew Warman; F Michael Pope; Andrea Superti-Furga; P Andrew Futreal; Nazneen Rahman
Journal:  Am J Hum Genet       Date:  2003-08-21       Impact factor: 11.025

4.  The gene for juvenile hyaline fibromatosis maps to chromosome 4q21.

Authors:  Nazneen Rahman; Melanie Dunstan; M Dawn Teare; Sandra Hanks; Sarah J Edkins; Jaime Hughes; Graham R Bignell; Grazia Mancini; Wim Kleijer; Mary Campbell; Gokhan Keser; Carol Black; Nigel Williams; Laura Arbour; Matthew Warman; Andrea Superti-Furga; P Andrew Futreal; F Michael Pope
Journal:  Am J Hum Genet       Date:  2002-09-04       Impact factor: 11.025

5.  Infantile systemic hyalinosis: A case report and review of literature.

Authors:  Bhushan Madke; Vidya Kharkar; Sunanda Mahajan; Siddhi Chikhalkar; Uday Khopkar
Journal:  Indian Dermatol Online J       Date:  2010-07

6.  Infantile Systemic Hyalinosis: Report of 17-year Experience.

Authors:  Seyed Reza Raeeskarami; Yahya Aghighi; Azadeh Afshin; Abdolreza Malek; Ali Zamani; Vahid Ziaee
Journal:  Iran J Pediatr       Date:  2014-12-09       Impact factor: 0.364

7.  Infantile systemic hyalinosis: Variable grades of severity.

Authors:  Ali Al Kaissi; Marwa Hilmi; Zulfiya Betadolova; Sami Bouchoucha; Svetlana Trofimova; Mohammad Shboul; Guseyn Rustamov; Wiam Dwera; Katharina Sigl; Vladimir Kenis; Susanne Gerit Kircher
Journal:  Afr J Paediatr Surg       Date:  2021 Oct-Dec
  7 in total

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